US4673565A - Pharmaceutical compositions containing hollow fine tubular drug delivery systems - Google Patents

Pharmaceutical compositions containing hollow fine tubular drug delivery systems Download PDF

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US4673565A
US4673565A US06730064 US73006485A US4673565A US 4673565 A US4673565 A US 4673565A US 06730064 US06730064 US 06730064 US 73006485 A US73006485 A US 73006485A US 4673565 A US4673565 A US 4673565A
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tube
composition
drug
tubes
polymer
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Robert C. Di Luccio
Ray B. Duggins
Eli Shefter
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Bristol-Myers Squibb Pharma Co
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E I du Pont de Nemours and Co
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0092Hollow drug-filled fibres, tubes of the core-shell type, coated fibres, coated rods, microtubules, nanotubes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/70Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S514/00Drug, bio-affecting and body treating compositions
    • Y10S514/964Sustained or differential release type
    • Y10S514/965Discrete particles in supporting matrix

Abstract

Pharmaceutical compositions are provided which contain hollow fine tube drug delivery systems. The compositions comprise a pharmaceutically suitable carrier, preferably in the form of a capsule, tablet, suspension, or suppository, and at least one drug delivery system which consists essentially of (1) a polymeric tube having a membrane outer sheath and a hollow core, and (2) at least one drug compound contained within the core, said system contained in the composition in an amount sufficient to deliver a therapeutic amount of the drug contained therein at a predetermined rate over a predetermined period of time. By varying the polymer, the permeability of the outer sheath, the drug, the drug concentration in the hollow core of the tube, the tube diameter, the tube length, the tube core diameter, and the sealing of the tube ends, a wide variety of drug therapeutic amounts, rates and dosing times can be achieved.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to pharmaceutical compositions and more particularly to controlled release pharmaceutical compositions containing hollow tube drug delivery systems.

2. Prior Art

Controlled delivery or sustained release formulations have gained wide popularity in the pharmaceutical industry. The popularity of these formulations has grown due to the usefulness in extending the utility of particular drugs which require specific dosages and delivery of the dosage at a non-toxicological rate.

In the pharmaceutical industry, sustained release has been used extensively for oral medications over a number of years. Sustained release formulations include encapsulated pellets or beads, enteric coated formulations, use of slightly soluble salts, drug complexes, and porous tablets containing dispersed drugs.

Controlled drug delivery on the other hand is aimed at achieving sustained release of a drug at a constant rate (zero order) for long periods of time. Zero order release can be provided at the present time only by mechanical pumps, such as automatic syringes and implantable pumps, osmotic pumps such as Alza's systems known as Alzet®, Progestasert® and Ocusert®, chemically controlled biodegradable mechanisms, and diffusional systems based on polymeric membranes and matrices such as the currently marketed transdermal systems for the delivery of nitroglycerin for angina pectoris and scopolamine for motion sickness.

Solid fibers have been used in sutures encapsulated with antibiotics and in intrauterine devices to release hormones.

While much work has been done over many years relating to the sustained release and the controlled release of drugs, there still is a need for new systems that are capable of delivering a predetermined amount of a drug at a predetermined rate, over a selected time. The present invention provides such systems.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 schematically illustrates a procedure for preparing hollow tubes having drugs incorporated in the cores of the tubes via solutions of the drugs.

FIGS. 2 and 3 illustrate procedure involving membrane formation by utilization of density gradients. If the bath density is less than the tube, the tube will sink and collect at the bottom of the bath (FIG. 2). If the bath density is greater, the spinning device is inverted and the tube will float upward and collect at the top of the phase inversion stage (FIG. 3).

SUMMARY OF THE INVENTION

According to the present invention there is provided a pharmaceutical composition comprising a pharmaceutically suitable carrier and at least one drug delivery system consisting essentially of (1) a polymeric fine tube having a membrane outer sheath and a hollow core, and (2) at least one drug compound contained within the core, said system contained in the composition in an amount sufficient to delivery a therapeutic amount of the drug contained therein at a predetermined rate over a predetermined period of time.

According to a preferred embodiment, a plurality of hollow, porous, segmented polyurethane/urea tubes up to 15 cm in length containing at least one drug in the core are contained in a pharmaceutical composition in the form of a tablet, capsule, suspension, suppository, or suture.

DETAILED DESCRIPTION OF THE INVENTION

The preparation of hollow tubes from polymers can be achieved by various routes. These are referred to as wet, dry or melt-forming processes. Melt-forming involves heating a polymer above its melting point and extruding it through an orifice (usually referred to as a die) which is designed to form a hollow tube. Once extruded, the melt is cooled via a quench which allows the polymer to solidify into a fine tube. In the dry-forming process, a solution of the polymer is extruded through a desired orifice and is fed into a heated column which allows for evaporation of the solvent and subsequent formation of a tube. In a wet-membrane forming process, a solution of the polymer is extruded though an orifice and quenched in a non-solvent for the polymer resulting in coagulation of the polymer to a tube. Of the above mentioned forming processes, wet-membrane forming allows one to easily produce hollow porous tubes. It will be appreciated that the particular forming process used will be dependent upon the polymer used and type of hollow tube desired.

To make a membrane outer sheath in a hollow tube, one first dissolves or disperses a polymer to form a liquid solution. A porous membrane results when the latter process is reversed under controlled condition. The polymer coagulates into a continuous matrix as it separates from the solvent which forms a dispersion of droplets. As the polymer solidifies and the solvent is extracted, the dispersion of droplets becomes a network of open pores. This phase inversion or separation can be achieved by a number of techniques. In one, the temperature of the polymer solvent dictates the point at which the phase inversion occurs. In another, the polymer solvent is physically exchanged with a poor solvent for the polymer causing phase inversion.

The size of the pores is affected by the solvent strength of a polymer. A rapid decrease in solvent strength often tends to entrap a dispersion of small droplets within the continuous polymer phase. A slow decrease in solvent strength allows for nucleation sites within the polymer matrix allowing for formation of larger pores. In this case, the reduction in solvent strength must be rapid enough to allow for the structure of the membrane to set.

Another way to change porosity and volume of the porous network in the polymer is to change the concentration of the polymer solution. Lower concentrations have a tendency to promote larger pores and greater pore volume. However, there is a limit to how high (usually no more than 45% w/w) the polymer concentration can be in a solvent, otherwise, the polymer will become the dispersed phase in a continuous solvent phase, thereby eliminating the porous network. Another method to achieve porous tubular membranes is to cause a rapid phase inversion of the polymer solution by cooling.

Generally, as the polymer membrane of the hollow tube is quenched, the surface of the polymer tends to have a "dense" skin due to a rapid reduction of solvent strength at the surface. The interior, on the other hand, must have the solvent diffuse and migrate through the polymer matrix. This results in larger interior pores. In a thermally induced quench, the relative cooling rates can determine the relative degree of porosity.

Conventional machinery used in the manufacture of tubes often has a tendency to orient the polymer by either the mechanical features of the device or by the influence of gravity. This often results in distortion of pore shape and orientation in tubular membrane production and also requires that the solution have inherent physical properties enabling it to be processed on the conventional equipment. Hot and cold drawing can also be used to vary the outside diameter of the tube and its core volume. For example, a large diameter tube can be extruded and then drawn down to a small diameter.

In order to minimize the effects of orientation and maximize the benefits of uniform porosity and allow for production of membranes from fragile polymer systems, a preferred tube forming process called density gradient membrane formation is used. This process uses density gradients in the phase inversion bath. Careful selection of the coagulation solutions allows one to use gravity to gently draw and collect the thin tubular membrane in the phase inversion bath. The density gradient of the coagulation solution can be established by either multiple stacked layers of liquids with different densities, or by the use of a single coagulant subject to a temperature gradient which in turn produces a density gradient. Proper selection of the coagulation solution is extremely important when processing delicate membranes. Depending on the density of the tube vs. the quench bath, it can be spun either upwards or downwards. For drug encapsulation, selection of the quench media is dependent on the drug solubility and miscibility of the solvent for the polymer.

In order to encapsulate a drug compound in the core of the hollow tube, either a suspension, solution, or other extrudable form of the compound has to be prepared initially. This is achieved by selecting a solvent for the drug and dissolving it to a desired concentration or by melting the drug material to be encapsulated. Alternatively, a suspension of fine particles of drug in an appropriate liquid medium is prepared which can either be heated to form a liquid suspension that can be solidified in the core of the tube or can be made viscous enough for the drug to remain in suspension. Often a dilute solution of the polymer used to make the tubular membrane outer sheath serves as an adequate suspending medium for the drug. Once the appropriate drug solution or suspension is made, it is pumped into the annular die simultaneously with the solution of the polymer forming the outer sheath of the hollow tube. This is schematically illustrated in FIG. 1. The resulting hollow tube containing the drug is quenched in an appropriate poor solvent for the polymer and the drug and is permitted to set in the quench bath. If necessary, the tube can be removed from the initial quench and placed in another solvent which can expedite removal of the remaining solvent in the tube, without removing the drug. For example, a volatile non-solvent for the drug and tube can be used to exchange with any residual solvent remaining in the tube and subsequently be removed by vacuum extraction.

After the drug encapsulated hollow tube is formed, the continuous tube is cut into lengths suitable for formulation into a pharmaceutical composition for administration to mammals, particularly in the form of a tablet, capsule, suppository, suspension, or suture. The length of the hollow tube can be as long as can conveniently be formulated into a dosage form commensurate with the delivery of a therapeutic amount of the encapsulated drug. Formulations can be prepared making use of carriers, vehicles, diluents; excipients, and procedures well known to those skilled in the pharmacy art.

For example, the hollow tubular delivery system can be one continuous length that can be "balled up" into a dosage form. The continuous tube may be more suitable for the slow release of a drug over a long period of time via an osmotic pump delivery system. In this delivery system, at least one of the tube ends is open and the membrane outer sheath is impermeable to water and the drug, i.e., the drug is delivered out the end of the tube. Release rates can be increased by making the membrane outer sheath permeable or semi-permeable.

Preferred pharmaceutical compositions contain a plurality of drug encapsulated hollow tubes. These tubes can be of uniform length or of different lengths with the ends either open or sealed. By varying the lengths of the tubes, openness of the ends, the permeability of the membrane outer sheath, the rate and time of delivery can be varied and be predetermined. Tube lengths up to 15 cm are preferred; however, shorter lengths are more preferred, e.g., the tubes are preferably less than 2 cm long, preferably in the range of less than about 0.5 mm to about 2 cm, and most preferably in the range of about 0.5 mm to about 6 mm. The tubes can have both ends open, both ends sealed, or one end open and one end sealed.

The hollow tubes preferably have a small diameter for ease of formulation. While final diameters can be as high as 5 mm, it is preferred that they be about 0.5 mm in outside diameter or less. Larger diameter tubes can be spun and then drawn down to a smaller diameter. Aspect ratios (ratio of length to diameter) of the tubes will generally be in the range of about 1 to 30. The core diameters of the hollow tubes typically range from about 25%-90% of the outside diameter, preferably about 40% to 85%.

The drug concentration in the core of the tube depends upon many variables and will be loaded to provide the best delivery rate and time span for the particular drug involved. Drug concentration can vary over a wide range, i.e., about 1-90% by weight of the total weight of the tube and compound; however, it is preferred that the drug concentration be in the range of about 5 to 75% by weight.

The drug in the core can be mixed with a pharmaceutically suitable salt or sugar to increase the dissolution of the drug in the core. This is particularly appropriate where the tube acts as an osmotic pump since the salt or sugar assists in forcing water into the core. While magnesium sulfate is a preferred salt, other useful salts are any water-soluble, divalent or monovalent salts.

A hollow tube that has been found particularly suitable for pharmaceutical formulations is a segmented polyurethane/urea tube free of additives having an outside diameter of less than 0.5 to about 1.5 mm, a core volume of about 60-90%, a length of about 3-6 mm and a drug concentration in the range of about 25-75% by weight. The membrane outer sheath of these tubes is porous, and had a porosity of 500 daltons or more, determined by dye penetration tests.

The material of choice for production of the hollow tube depends on the characteristics one would like to have in the final product. They can be chosen for ease of membrane fabrication, hydrophilicity, elasticity, molecular weight, biocompatibility, degree of porosity, processing temperature, and compatibility with the drug being encapsulated. Polymers which can be used include polyolefins such as polypropylene, polyurethanes such as segmented polyurethane/ureas, ethylene-vinyl acetate copolymers having a vinyl acetate content of at least 33% by weight, polyvinyl alcohols, and blends of water-soluble polymers with some of the aforementioned polymers.

Polypropylene can be used for the production of fine hollow tubular membranes with wide variations in porosity. They are normally melt formed at temperature above 200° C. but they can also be dissolved in solvents at elevated temperatures and then quenched. Because of the high temperatures necessary for the fabrication of polypropylene hollow tubes, care must be used in selecting drugs which are not heat sensitive. Alternatively, the drug can be injected into the core of the hollow tube after it is formed; however, such a procedure is not preferred.

Polyurethanes, such as segmented polyurethane/ureas sold under the name Lycra®, can be dissolved at ambient temperature in dimethylacetamide (DMAC) or other appropriate solvent and fabricated into porous, hollow tubes at ambient temperature. They can also be blended easily with water-soluble materials such as polyvinylpyrrolidone (PVP), polyethylene glycol (PEG), and salts which enhance porosity and wettability of the resulting tubular membrane. These tubes have high elasticity, are biocompatible, and offer great flexibility in the design of hollow tubular membranes, especially by the preferred density gradient membrane formation technique. Copolymers of ethylene-vinyl acetate with at least 33% by weight of vinyl acetate can be dissolved at ambient temperature in tetrahydrofuran (THF) and fabricated into porous hollow tubes. They are easily blended with water soluble materials such as PVP, PEG, and salts. These tubular membrane systems are somewhat elastic, are biocompatible, and are easily formed into hollow tubes. Hytrel®, a polyester elastomer, can also be formed into porous tubular membranes and blended with water-soluble polymers.

Polyvinyl alcohols can be dissolved easily in hot water at 60° C. and can be fabricated into porous hollow tubes at ambient temperatures. Because of their solubility in water, they can be used as slowly erodible matrixes for delivery of active ingredients.

Any therapeutically active drug compound can be used. In the examples which follow, the following compounds were chosen as models because of their broad range of chemical and pharmacological characteristics:

Phenylpropanolamine hydrochloride, a decongestant, pKa (base)=9.5, is freely soluble in water (25° C.).

Theophylline, an antiasthma drug, pKa (base)=0.36 with a solubility in water of 1 gram in 120 mls (25° C.).

Chlorpheniramine maleate, an antihistamine, pKa (base)=8.99, has a solubility of 1 gram in 3.4 ml water (25° C.).

Salicyclic acid, a topical antiseptic, pKa=2.97, is slightly soluble in water.

Indomethacin, an antiinflammatory drug, pKa (acid)=4.5, has a low solubility in water.

Nalbuphine hydrochloride, an analgesic, pKa (base)=8.4, is soluble in water.

In the Examples which follow, hollow tubes were prepared by one of two procedures which can be varied depending upon the end results desired. Drugs were incorporated in the cores of the tubes via solutions or suspensions of the drugs.

Procedure A

This procedure uses the arrangement shown in FIG. 1. In this procedure, a solution of the polymer for the outer membrane sheath is pumped through the annular die simultaneously with a solution of the core material which results in a tubular membrane surrounding core solution. This is passed through an annular die (O.D.=2.18 mm) into a quench tube containing 1 liter of a coagulant for the polymer. The solvent is continuously removed from the polymer/drug encapsulated system and it is collected in a rotating piddle pot. The loaded tube remains in the piddle pot as the solvent is being removed and is removed after solvent removal is nearly complete for further treatment, e.g., removal of trace amounts of solvent. The tube is formed at a rate of 0.1 to 2 cm3 /min and the speed of the piddle pot is the same as the speed of the tube as it exists the quench tube. Temperature of spinning and coagulation are controlled by heating mantles surrounding the die and coagulation kettle.

Table I gives Examples of drug loaded tubes which were formed by the above method. All runs were conducted at room temperature.

Procedure B

This procedure involves membrane formation by utilization of density gradients. This procedure is desirable for most applications where membrane fabrication and drug encapsulation are involved. Due to excessive "draw" which is inherent in most extrusion techniques and also to the difficulty of fabricating slow forming membranes or tubes whose polymer structure has weak physical characteristics, this procedure allows for membrane formation of polymers having any or all of the characteristics mentioned. By correctly choosing coagulants with a density slightly different than that of the polymer/drug encapsulated tube, one can use gravity to gently draw and collect a forming tube within the phase inversion bath (coagulant). If the bath density is less than the tube, the tube will sink and collect at the bottom of the bath (FIG. 2). If the bath density is greater, the spinning device is inverted and the tube will float upward and collect at the top of the phase inversion stage (FIG. 3). This procedure can use several bath fluids of decreasing density stacked vertically in the tube allowing for flexibility in design to give the ability to use a sequence of quench-coagulation treatments in the same phase inversion unit. For example, a layer of a heavy liquid can be placed adjacent to the die for thermal insulation. A lighter heat conductive liquid on top of this layer becomes the quenching agent.

The encapsulation of drugs is accomplished by dissolving or suspending the drug in a suitable liquid, or melting the drug, then taking this drug preparation and loading it into a stainless steel piston used for inserting the core material. A second piston for the outer sheath membrane contains the polymer solution. Temperature control, if necessary, of the pistons, die, and coagulant is accomplished by heating jackets. Die size is chosen depending on the diameter of the tube desired, and on the lumen desired. The rate at which the polymer and drug is pumped is controlled by settings on the pumps. The gap between the die and the top of the coagulation bath, where appropriate, is set according to the amount of "drawn down" desired.

In Tables I and II are given the conditions and characteristics of the tubes prepared using this procedure. All parts and percentages are by weight.

The following abbreviations are used in the tables:

Polymers and solvents:

Ur126=Segmented polyurethane/urea (50,000 molecular weight)

PVP-15=Polyvinylpyrrolidone (15,000 molecular weight; 40=40,000 molecular weight)

PEG=Polyethylene glycol (400 molecular weight; 740 molecular weight; 1000 molecular weight; 1300 molecular weight; 3350 molecular weight)

PG=Propylene glycol

EVA=Copolymer of ethylene-vinyl acetate with 33% by weight vinyl-acetate (melt index 43, density 0.95 g/cc)

NMP=1-Methyl-2-pyrrolidone

DMAC=Dimethylacetamide

THF=Tetrahydrofuran

Dowex=Dowex 50 cross-linked sulfonated polystyrene ion exchange resin

Drugs

Sal. Acid=Salicyclic acid

PPA=Phenylpropanolamine hydrochloride

CM=Chlorpheniramine Maleate

Nalb--HCl=Nalbuphine hydrochloride

Theo=Theophylline

Ind=Indomethacin

                                  TABLE I__________________________________________________________________________Hollow Thin Tubular MembranePreparation With Encapsulated Drugs                          Direction          Core %     Air  ofEx.   Polymer     in Susp.   Gap  MembraneNo.   (Solvent)   or Soln.   (Inches)                          Formation                               Quench__________________________________________________________________________1  36% Ur126 (DMAC)          3% Theo in PG                     0    A    H.sub.2 O2  36% Ur126 (DMAC)          10% Sal. Acid                     0    A    H.sub.2 O          in PG3  36% Ur126 (DMAC)          3% Theo in PG                     0    A    H.sub.2 O4  36% Ur126 (DMAC)          30% Sal. Acid                     0    A    H.sub.2 O          in PEG 7405  36% Ur126 (DMAC)          30% Sal. Acid                     0    A    H.sub.2 O          in PEG 10006  36% Ur126 (DMAC)          30% Sal. Acid                     0    A    H.sub.2 O          in PEG 13007  36% Ur126 (DMAC)          25% Ind. in                     1    B(down)                               60%          PEG 3350             Ethanol                               in H.sub.2 O8  36% Ur126 (DMAC)          50% Nalb-HCl in                     1/4  B(down)                               60%          3.6% Ur (DMAC)       Ethanol                               in H.sub.2 O9  36% Ur126 (DMAC)          50% Nalb-HCl in                     1/4  B(down)                               60%          3.6% Ur (DMAC)       Ethanol                               in H.sub.2 O10 36% Ur126 with          25% Nalb-HCl in                     1/4  B(down)                               60%   15% PVP40 (DMAC)          1.8% Ur126 in        Ethanol          DMAC                 in H.sub.2 O11 36% (Ur126 +          25% Nalb-HCl in                     1/4  B(down)                               60%   25% PVP-15)(DMAC)          1.8% Ur126 in        Ethanol          DMAC                 in H.sub.2 O12 36% Ur126 (DMAC)          25% Nalb-HCl in                     1/4  B(down)                               60%          1.8% Ur126 in        Ethanol          DMAC                 in H.sub.2 O13 15% Elvanol 50% PPA in 0    B(down)                               60%   HV (H.sub.2 O)          2% Elvanol in        Ethanol          H.sub.2 O            in H.sub.2 O14 20% EVA 150 (THF)          25% Theo in                     1/2  B(down)                               60%          3.6% Ur126 (DMAC)    Ethanol                               in H.sub.2 O15 36% (Ur126 +          25% Theo in                     0    B(down)                               60%   25% PVP-15)(DMAC)          3.6% Ur126 (DMAC)    Ethanol                               in H.sub.2 O16 Polypropylene          33% Theo   Not spun (encapsulated          325 mesh in 3.6%                     in previously prepared          Ur126 (DMAC)                     tube17 36% Ur126   50% CM in  1    B(down)                               80%          3.6% Ur126 (DMAC)    Acetone                               in H.sub.2 O18 36% (Ur126: 33% (PPA-Dowex)                     0    B(up)                               Deionized   PVP-15, 1:1)          in 3.6% Ur126        Distilled          (DMAC)               Water__________________________________________________________________________

In vitro dissolution rates of drug-filled hollow tubes whose preparation is shown in Table I were carried out by one of two procedures. One is a standard procedure described in the U.S. Pharmacopeia XXI, page 1243 (1985). This procedure uses a 1 liter glass vessel immersed in water at 30° C. or 37° C. and filled with a specified amount of drug encapsulated tubes and an appropriate dissolution medium (0,1N HCl, pH 7.4 phosphate buffer, buffered saline or water). This vessel is stirred at a constant rate (25, 50 or 100 rpm) for the duration of the dissolution procedure and its contents are sampled periodically to determine the amount of drug released.

The second procedure, sometimes referred to as the rotating bottle method, uses sealed, cylindrical glass tubes immersed in water at 30° C. or 37° C. and filled with drug encapsulated tubes and an appropriate dissolution medium as described above. The glass tubes are tumbled at a specified rate (15 rpm) throughout the test and the contents are sampled periodically to determine the amount of drug released. The length of the tests vary depending on the rate of release of the drug (2-100 hours). Time should be long enough to allow significant (˜>50%) release of drug.

The in vitro dissolution procedures of Table I hollow tubes are shown in Table II along with the characteristics of the tubes. The dissolution results are discussed after Table II.

                                  TABLE II__________________________________________________________________________Drug-encapsulated Thin TubularMembranes And Dissolution Rates               Tube      Drug   Mem- Drug &      Dia.      LoadingEx.   brane   Susp.  Tube (OD       Ult. %                              Dissol.No.   Sheath   Agent  Length               mm.)                  Char.  of Total                              Proc.__________________________________________________________________________1  Ur126   3% Theo.          1"   1.5                  Closed  2%  USP 30° C./   in PG  (2.54 cm)                  ends 70%    50 rpm.sup.1                  Lumen Dia.2  Ur126   10% sal.          1"   1.5                  Closed 6.9% USP 30° C./   acid in          (2.54 cm)                  ends 70%    50 rpm.sup.1   PG             Lumen Dia.3  Ur126   3% Theo.          1"   1.5                  Closed  2%  rot. bottle   in PG  (2.54 cm)                  ends 60%    37° C./                  Lumen Dia.  15 rpm.sup.14  Ur126   30% sal.          1"   3.6                  Closed 12%  rot. bottle   acid in          (2.54 cm)                  ends 67%    30° C./   PEG 740        Lumen Dia.  15 rpm.sup.15  Ur126   30% sal.          1"   3.0                  Closed 22%  rot. bottle   acid in          (2.54 cm)                  ends 33%    30° C./   PEG 1000       Lumen Dia.  15 rpm.sup.16  Ur126   30% sal.          1"   3.0                  Closed   20.2%                              rot. bottle   acid in          (2.54 cm)                  ends 33%    30° C./   PEG 1300       Lumen Dia.  15 rpm.sup.17  Ur126   25% Ind.          1"   2.3                  Closed 17%  USP 37° C./   in PEG (2.54 cm)                  ends 33%    25 rpm.sup.1   3350           Lumen Dia.8  Ur126   50:3.6 1"   1.8                  Closed and                         56%  USP 37° C./   Nalb-HCl:          (2.54 cm)                  open 82%    50 rpm.sup.2   Ur126          Lumen Dia.9  Ur126   50:3.6 1/2",               1  Open -50%                           39.8%                              USP 37° C./   Nalb-HCl:          1"      Lumen Dia.  50 rpm.sup.2   Ur126  (1.27,          2.54 cm)10 Ur126   25:1.8 1"   1  Open and                         40%  USP 37° C./   & 15%   Nalb-HCl:          (2.54 cm)                  closed 50%  50 rpm.sup.2   PVP-40   Ur126          Lumen Dia.11 Ur126   25:1.8 1"   1  Open and                         56%  USP 37° C./   & 25%   Nalb-HCl:          (2.54 cm)                  closed 67%  50 rpm.sup.2   PVP-15   Ur126          Lumen Dia.12 Ur126   25:1.8 1"   1  Open and                         66%  USP 37° C./   Nalb-HCl:          (2.54 cm)                  closed 74%  50 rpm.sup.2   Ur126          Lumen Dia.13 Elvanol   50:2 PPA:          1"   0.8                  Closed ends                         28%  USP 37° C./   HV   Elvanol          (2.54 cm)                  40% Lumen   100 rpm.sup.2   HV14 EVA 150   25:3.6 1"   0.8                  Closed ends                         30%  USP 37° C./   Theo:Ur126          (2.54 cm)                  35% Lumen   100 rpm.sup.215 Ur126   25:3.6 1"   1.2                  Closed ends                         51%  USP 37° C./   & 25%   Theo:  (2.54 cm)                  40% Lumen   100 rpm.sup.2   PVP-15   Ur12616 Poly-   33:3.6 1"   1.2                  Closed ends                         25%  USP 37° C./   propyl-   Theo:  (2.54, cm)                  37% Lumen   100 rpm.sup.2   ene  Ur12617 Ur126   50:3.6 1/8",               0.9                  Open ends                         28%  USP 37° C./   CM:Ur126          1/2"    75% Lumen   100 rpm.sup.2          (0.32 cm,          1.27 cm)18 1:1  33:3.6 1/8",               0.68                  Open Ends                         57%  USP 37° C./   Ur126:   PPA-Dowex          1/4",   86% Lumen   100 rpm.sup.3   PVP-15   Ur126  1/2"          (0.32, 0.64,          1.27 cm)__________________________________________________________________________ .sup.1 0.05 M pH 7.4 phosphate buffer .sup.2 distilled water .sup.3 0.1 NHCl

The drug release patterns obtained with the pharmaceutical compositions of this invention can be further understood by reference to the following examples in which temperatures are in degrees centigrade.

EXAMPLE 1

The dissolution of theophylline from hollow porous polyurethane tubes containing 2% theophylline by weight was determined in pH 7.4 phosphate buffer at 30° C. using the USP dissolution procedure. The tubes were prepared by encapsulating a 3% suspension of theophylline in propylene glycol in polyurethane 126 tubes prepared to have a 1.5 mm outside diameter with a 70% lumen diameter. The drug encapsulated tubes were cut in one inch lengths and both ends were closed. The dissolution bath was stirred at 50 rpm. During the first hour, about 25% of the theophylline was released, followed by a sustained release with about 80% of the total theophylline being released by 11 hours.

EXAMPLE 2

The dissolution of salicyclic acid from hollow porous polyurethane tubes containing 6.9% salicyclic acid by weight was determined in pH 7.4 phosphate buffer at 30° C. using the USP dissolution procedure. The tubes were prepared by encapsulating a 10% suspension of salicyclic acid in propylene glycol in polyurethane 126 tubular membranes prepared to have a 1.5 mm outside diameter with a 70% lumen diameter. The tubes were cut to one inch lengths and both ends were closed. The dissolution bath was stirred at 50 rpm. Rapid release of 60% of the salicylic acid was observed during the first hour, followed by complete release over 3 hours.

EXAMPLE 3

The dissolution of theophylline from hollow porous polyurethane tubes containing 2% theophylline by weight was determined in pH 7.4 phosphate buffer at 37° C. using the rotating bottle sustained release apparatus equipped with 50 ml bottles. The tubes were prepared by encapsulating a 3% suspension of theophylline in propylene glycol in polyurethane 126 tubular membranes prepared to have a 1.5 mm outside diameter with a 60% lumen diameter. The tubes were cut in one inch lengths and both ends were closed. The bottles were tumbled in the constant temperature bath at 10 rpm. During the first 1/2 hour. about 40% of the theophylline was released. followed by more constant release to give complete dissolution over 4 hours.

EXAMPLE 4

The dissolution of salicylic acid from hollow porous polyurethane tubes containing 12% salicylic acid by weight was determined in pH 7.4 phosphate buffer at 30° C. using the rotating bottle sustained release apparatus equipped with 50 ml bottles. The drug encapsulated tubes were prepared by encapsulating a 30% suspension of salicylic acid in polyethylene glycol 740 in polyurethane 126 tubes prepared to have a 3.6 mm outside diameter with a 67% lumen diameter. The tubes were cut in one inch lengths with both ends closed. The bottles were tumbled in the constant temperature bath at 15 rpm. During the first 1/2 hours, about 30% of the salicylic acid was released, followed by more constant release of 95% of the total salicylic acid over 6 hours.

EXAMPLE 5

The dissolution of salicylic acid from hollow porous polyurethane tubes containing 22% salicyclic acid by weight was determined in pH 7.4 phosphate buffer at 30° C. using the rotating bottle sustained release apparatus equipped with 50 ml bottles. The tubes were prepared by encapsulating a 30% suspension of salicylic acid in polyethylene glycol 1000 in polyurethane 126 membranes prepared to have a 3.0 mm outside diameter and a 33% lumen diameter. The tubes were cut in one inch lengths with both ends closed. The bottles were tumbled in the constant temperature bath at 15 rpm. During the first 1/2 hour, about 35% of the salicylic acid was released followed by more constant release of 95% of the total salicylic acid over 6 hours.

EXAMPLE 6

The dissolution of salicylic acid from hollow porous polyurethane tubes containing 20.2% salicyclic acid by weight was determined in pH 7.4 phosphate buffer at 30° C. using the rotating bottle sustained release apparatus equipped with 50 ml bottles. The tubes were prepared by encapsulating a 30% suspension of salicylic acid in polyethylene glycol 1300 in polyurethane tubes prepared to have a 3.0 mm outside diameter and a 33% lumen diameter. The drug loaded tubes were cut in one inch lengths with both ends closed. The bottles were tumbled in the constant temperature bath at 15 rpm. During the first 1/2 hour, about 40% of the salicyclic acid was released followed by more constant release of 78% of the total salicylic acid over 6 hours.

EXAMPLE 7

The dissolution of indomethacin from hollow porous polyurethane tubes containing 17% indomethacin by weight was determined in pH 7.4 phosphate buffer using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a 25% suspension of indomethacin in polyethylene glycol 3350 in polyurethane 126 tubular membranes prepared to have a 2.3 mm outside diameter with a 33% lumen diameter. The drug loaded tubes were cut in one inch lengths with both ends closed. The dissolution bath was stirred at 25 rpm. During the first 1/2 hour. about 42% of the indomethacin was released, followed by more constant release of about 85% of the total indomethacin over 11 hours.

EXAMPLE 8

The dissolution of nalbuphine hydrochloride from hollow porous polyurethane tubes containing 56% nalbuphine hydrochloride by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 50 parts nalbuphine hydrochloride to 3.6 parts polyurethane 126 in polyurethane 126 tubular membranes prepared to have a 1.8 mm outside diameter with a 82% lumen diameter. The drug encapsulated tubes were cut in one inch lengths with either both ends closed or both ends left open. The dissolution bath was stirred at 50 rpm. The open-ended tubes showed almost constant release of nalbuphine hydrochloride with complete release over 100 hours. The close-ended tubes showed almost constant release of nalbuphine hydrochloride; however, only about 25% of the total nalbuphine hydrochloride had been released after 100 hours.

EXAMPLE 9

The dissolution of nalbuphine hydrochloride from hollow porous polyurethane tubes containing 39.8% nalbuphine hydrochloride by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 50 parts nalbuphine hydrochloride to 3.6 parts polyurethane 126 in polyurethane 126 tubes prepared to have a 1 mm outside diameter and a 50% lumen diameter. The tubes were cut in one inch and in 1/2 inch lengths, giving tubular membranes having aspect ratios (length/diameter) of about 25 and 12.5 respectively. The ends of the drug encapsulated tubes were left open. The dissolution bath was stirred at 50 rpm. Both sets of tubes showed virtually constant release of nalbuphine hydrochloride with the tubes with an aspect ratio of 25 resulting in release of about 20% of the total nalbuphine hydrochloride over a 24 hour period while the tubes with an aspect ratio of 12.5 resulted in about 65% of the total nalbuphine hydrochloride being released over a 24 hour period.

EXAMPLE 10

The dissolution of nalbuphine hydrochloride from hollow porous polyurethane tubes containing 15% polyvinylpyrrolidone and 40% nalbuphine hydrochloride by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 25 parts nalbuphine hydrochloride and 1.8 parts polyurethane 126 in a tube containing 15% polyvinylpyrrolidone 40 in polyurethane 126 prepared to have a 1 mm outside diameter and a 50% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were either closed or left open. The dissolution bath was stirred at 50 rpm. The open-ended tubes showed an initial release of about 5% of the nalbuphine hydrochloride during the first 1/2 hour. followed by a sustained release of 40% of the total nalbuphine hydrochloride by 24 hours. The closed-ended tubes showed a rapid release of about 4.5% of the nalbuphine hydrochloride during the first 2 hours, followed by a more sustained release of 8% of the total nalbuphine hydrochloride by 24 hours.

EXAMPLE 11

The dissolution of nalbuphine hydrochloride from hollow porous polyurethane tubes containing 25% polyvinylpyrrolidone 15 and 56% nalbuphine hydrochloride by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 25 parts nalbuphine hydrochloride to 1.8 parts polyurethane 126 in a tube containing 25% polyvinylpyrrolidone 15 in polyurethane 126 prepared to have a 1 mm outside diameter and a 67% lumen diameter. The drug encapsulated tube was cut to one inch lengths and the ends were either closed or left open. The dissolution bath was stirred to 50 rpm. The open-ended tubes showed a fairly constant release with about 36% of the total nalbuphine hydrochloride being released in 24 hours. The tubes with the closed ends showed an initial release of about 5% of the nalbuphine hydrochloride during the first 1/2 hour, followed by sustained release to reach 10% of the total nalbuphine hydrochloride at 24 hours.

EXAMPLE 12

In contrast to the dissolution observed in Example 11a the dissolution of nalbuphine hydrochloride from hollow porous tubes of polyurethane alone, rather than the blended polymers used in Example 11, was found to be much slower. Tubes were prepared which contained 66% nalbuphine hydrochloride by weight by encapsulating a mixture of 25 parts nalbuphine hydrochloride and 1.8 parts polyurethane 126 in polyurethane 126 tubes with a 1 mm outside diameter and a 74% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were either closed or left open. The dissolution was determined under the same conditions as those used for Example 11. The open-ended tubes resulted in only 4% dissolution of the total nalbuphine hydrochloride at 24 hours, while the closed-ended tubes released only 1.5% of the total nalbuphine hydrochloride at 24 hours.

EXAMPLE 13

The dissolution of phenylpropanolamine hydrochloride from hollow porous Elvanol HV tubes containing 28% phenylpropanolamine hydrochloride by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 50 parts phenylpropanolamine hydrochloride and 2 parts Elvanol HV in an Elvanol HV tube prepared to have an outside diameter of 0.8 mm with a 40% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were closed. The dissolution bath was stirred at 100 rpm. Complete release of the phenylpropanolamine hydrochloride was observed in the first two hours.

EXAMPLE 14

The dissolution of theophylline from hollow ethylene vinyl acetate tubes containing 30% theophylline was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture containing 25 parts theophylline to 3.6 parts polyurethane 126 in a tubular membrane of ethylene-vinyl acetate copolymer (33% vinyl acetate by weight) prepared to have an outside diameter of 0.8 mm and a 35% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were closed. The dissolution bath was stirred at 100 rpm. After an initial release of about 20% of the theophylline during the first 1/2 hour, a constant release was observed resulting in complete release of the total theophylline by 24 hours.

EXAMPLE 15

The dissolution of theophylline from hollow porous polymethane tubes containing 25% polyvinylpyrrolidone and 51% theophylline by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture of 25 parts theophylline to 3.6 parts polyurethane 126 in a tubular membrane of polyurethane 126 polyvinylpyrrolidone 15 blend (25% polyvinylpyrrolidone) prepared to have an outside diameter of 1.2 mm with a 40% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were closed. The dissolution bath was stirred at 100 rpm. After an initial release of 20% of the theophylline in the first 15 minutes a constant release was observed with complete release of the theophylline by 24 hours.

EXAMPLE 16

The dissolution of theophylline from hollow polypropylene tubes with a mean wall porosity of <0.1 um containing 25% theophylline by weight was determined in water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture containing 33 parts theophylline to 3.6 parts polyurethane 126 in polypropylene tubes prepared to have an outside diameter of 1.2 mm and a 37% lumen diameter. The drug encapsulated tubes were cut to one inch lengths and the ends were closed. The dissolution bath was stirred at I100 rpm. After an initial release of 11% of the theophylline in the first 1-2 hour, sustained release was observed with 80% of the total theophylline being released by 24 hours.

EXAMPLE 17

The release of chlorpheniramine maleate from hollow porous polyurethane tubes containing 28% chlorpheniramine maleate by weight was determined in distilled water using the USP dissolution procedure at 37° C. The tubes were prepared by encapsulating a mixture containing 50 parts chlorpheniramine maleate to 3.6 parts polyurethane 126 in a polyurethane 126 tubular membrane prepared to have an outside diameter of 0.9 mm and a 75% lumen diameter. The drug encapsulated tubes were cut to lengths of 1/8 inch (0.32 cm) or 1/2 inch (1.27 cm), giving tubes with an aspect ratio of 1.4 or 5.6 respectively and the ends were left open. The dissolution bath was stirred at 100 rpm. The tubes with an aspect ratio of 1.4 showed an initial release of 22% of the chlorpheniramine maleate in the first 1/2 hour, followed by a sustained release to provide 85% of the total chlorpheniramine maleate at 8 hours. The tubes with an aspect ratio of 5.6 showed a constant release to provide 23% of the total chlorpheniramine maleate at 8 hours.

EXAMPLE 18

Release of phenylpropanolamine hydrochloride (PPA) from open-ended hollow tubes whose sheat is constructed of a 1:1 blend of urethane 126 and polyvinylpyrrolidone and with aspect ratios of from 4.6, 9.2, and 18.6 were performed in 0.1N HCl and compared to that obtained with the core material. The release pattern for the drug encapsulated tubes was sustained after an initial burst of 2, 3, and 6% (in <1/2 hour) and at 24 hours was about 42%, 60% and 70% for the small, medium, and low aspect ratio tubes respectively. The core component showed a fast release of PPA with a burst of 30% in <1/2 hour up to 100% in 20 hours.

Claims (16)

What is claimed is:
1. A pharmaceutical composition comprising:
a pharmaceutically suitable carrier and at least one drug delivery system consisting essentially of (1) a plurality of polymeric tubes having thin outer membrane sheaths and hollow cores, the length of each tube independently in the range of about 0.5 mm to about 5 cm, and (2) at least one solid, nonvaporizable drug compound contained within the cores, said system contained in the composition in an amount sufficient to deliver a therapeutic amount of the drug contained therein at a predetermined rate over a predetermined period of time.
2. The composition of claim 1 wherein the membrane outer sheath is impermeable and the tube ends are open.
3. The composition of claim 2 wherein the membrane outer sheath is permeable of semi-permeable.
4. The composition of claim 3 wherein 0 to 2 of the tube ends of each tube are sealed.
5. The composition of claim 1 wherein the core diameter is in the range of about 25%-90% of the outside diameter.
6. The composition of claim 1 wherein the drug compound concentration is in the range of about 1-90% by weight of the total weight of each tube and compound.
7. The composition of claim 5 wherein the concentration is in the range of about 5-75% by weight, and the length of each tube is independently in the range of less than 0.5 mm to about 6 mm, and whose aspect ratio is from about 1 to 30.
8. The composition of claim 5 wherein the membrane outer sheath of at least a portion of the tubes is permeable to water but not to the compound contained in the core, and these tubes have one end open and one end sealed.
9. The composition of claim 8 wherein the compound in the core is mixed with a pharmaceutically suitable salt or sugar.
10. The composition of claim 1 in the form of a capsule, tablet, or suppository.
11. The composition of claim 1 wherein the polymeric tube is formed from a polyolefin, a polyurethane, a copolymer of ethylene and vinyl acetate having at least 33% by weight vinyl acetate, a polyvinyl alcohol, or a blend of one of the aforesaid with a water-soluble polymer or salt.
12. The composition of claim 11 wherein the polymer is polypropylene having a melt index above 30 g/10 min and a solubility in hexadecylamine solvent above 20% w/w.
13. The composition system of claim 11 wherein the polymer is an ethylene-vinyl acetate copolymer having a melt index above 30 g/10 min and a solubility in a hydrocarbon solvent above 20% w/w.
14. The composition of claim 11 wherein the polymer is a segmented polyurethane/urea derived from polyether glycol soft segment containing no extra additives and soluble to greater than 30% w/w in dimethylacetamide or N-methylpyrrolidone.
15. The composition of claim 11 where the polymer is an ethylene-vinyl acetate copolymer blended with about 5 to 30% by weight of polyvinylpyrrolidone having a number average molecular weight of 15,000-40,000 or polyethylene glycol having a number average molecular weight of 400-20,000.
16. The composition of claim 14 wherein the polyurethane is a blend with about 5-50% by weight of polyvinylpyrrolidone having a number average molecular weight of 15,000-40,000 or polyethylene glycol having a number average molecular weight of 400-20,000.
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Controlled Release Society Meeting, Jul. 23 25, 1984, Ft. Lauderdale, FL. *
Controlled Release Society Meeting, Jul. 23-25, 1984, Ft. Lauderdale, FL.

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US5150718A (en) * 1987-08-08 1992-09-29 Akzo N.V. Method of contraception
US4957119A (en) * 1987-08-08 1990-09-18 Akzo N.V. Contraceptive implant
US5232438A (en) * 1988-10-03 1993-08-03 Alza Corporation Membrane for electrotransport transdermal drug delivery
US5080646A (en) * 1988-10-03 1992-01-14 Alza Corporation Membrane for electrotransport transdermal drug delivery
US5169383A (en) * 1988-10-03 1992-12-08 Alza Corporation Control membrane for electrotransport drug delivery
US5169382A (en) * 1988-10-03 1992-12-08 Alza Corporation Membrane for electrotransport transdermal drug delivery
US5147296A (en) * 1988-10-03 1992-09-15 Alza Corporation Membrane for electrotransport transdermal drug delivery
US5322502A (en) * 1988-10-03 1994-06-21 Alza Corporation Membrane for electrotransport transdermal drug delivery
WO1990012511A1 (en) * 1989-04-19 1990-11-01 Wm. Wrigley Jr. Company Gradual release structures for chewing gum
US5165944A (en) * 1989-04-19 1992-11-24 Wm. Wrigley Jr. Company Gradual release structures for chewing gum
US5154939A (en) * 1989-04-19 1992-10-13 Wm. Wrigley Jr. Company Use of salt to improve extrusion encapsulation of chewing gum ingredients
US5108762A (en) * 1989-04-19 1992-04-28 Wm. Wrigley Jr. Company Gradual release structures for chewing gum
US5198251A (en) * 1989-04-19 1993-03-30 Wm. Wrigley Jr. Company Gradual release structures for chewing gum
US5229148A (en) * 1989-04-19 1993-07-20 Wm. Wrigley Jr. Company Method of combining active ingredients with polyvinyl acetates
US4978537A (en) * 1989-04-19 1990-12-18 Wm. Wrigley Jr. Company Gradual release structures for chewing gum
US5364627A (en) * 1989-10-10 1994-11-15 Wm. Wrigley Jr. Company Gradual release structures made from fiber spinning techniques
US5683719A (en) * 1990-11-22 1997-11-04 British Technology Group Limited Controlled release compositions
US5128155A (en) * 1990-12-20 1992-07-07 Wm. Wrigley Jr. Company Flavor releasing structures for chewing gum
US5282829A (en) * 1991-08-15 1994-02-01 United States Surgical Corporation Hollow body implants
US5429822A (en) * 1992-03-13 1995-07-04 Cambridge Scientific, Inc. Biodegradable bursting release system
US5443461A (en) * 1993-08-31 1995-08-22 Alza Corporation Segmented device for simultaneous delivery of multiple beneficial agents
US8586083B2 (en) * 2002-06-18 2013-11-19 Euro-Celtique S.A. Gastroretentive drug delivery system comprising an extruded hydratable polymer
US20090324694A1 (en) * 2002-06-18 2009-12-31 Euro-Celtique, S.A. Gastroretentive drug delivery system comprising an extruded hydratable polymer
US20050125035A1 (en) * 2003-12-04 2005-06-09 Cichocki Frank R.Jr. Active suture for the delivery of therapeutic fluids
US20050125034A1 (en) * 2003-12-04 2005-06-09 Cichocki Frank R.Jr. Active suture for the delivery of therapeutic fluids
US20060030883A1 (en) * 2003-12-04 2006-02-09 Cichocki Frank R Jr Device for creating and maintaining infusion passages in tissue
US7875055B2 (en) 2003-12-04 2011-01-25 Ethicon, Inc. Active suture for the delivery of therapeutic fluids
US8128656B2 (en) 2003-12-04 2012-03-06 Ethicon, Inc. Device for creating and maintaining infusion passages in tissue
US8257393B2 (en) 2003-12-04 2012-09-04 Ethicon, Inc. Active suture for the delivery of therapeutic fluids
US20070207089A1 (en) * 2004-03-30 2007-09-06 Osvaldo Abreu Tamper Resistant Dosage Form Comprising an Adsorbent and an Adverse Agent
US8298579B2 (en) 2004-03-30 2012-10-30 Euro-Celtique S.A. Tamper resistant dosage form comprising an adsorbent and an adverse agent
US9795681B2 (en) 2004-03-30 2017-10-24 Purdue Pharma L.P. Tamper resistant dosage form comprising an adsorbent and an adverse agent

Also Published As

Publication number Publication date Type
JPS61268615A (en) 1986-11-28 application
EP0200224B1 (en) 1992-03-18 grant
CA1284105C (en) 1991-05-14 grant
DE3684354D1 (en) 1992-04-23 grant
EP0200224A3 (en) 1987-07-22 application
EP0200224A2 (en) 1986-11-05 application

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